Import Authorization

Workflow steps

1. Import Intent
   Private import intent alongside SCFM supply. SCFM is the primary domestic supplier but cannot meet demand — private imports are permitted and necessary to fill the supply gap. EU-GMP Part I required — Italy is EEA; AIFA issues EU-GMP certificates.
   • AIFA import authorization per shipment
   • Italian licensed importer
   • EU-GMP Part I mandatory
2. Apply: AIFA Per-Shipment Import Auth
   Per-shipment import authorization application to AIFA. Processing approximately 4–6 weeks. SCFM is the primary domestic supplier but private imports are also permitted.
   • EU-GMP Part I certificate
   • GACP certificate
   • COA per batch
   • Exporting country export authorization
   • Italian licensed importer as sponsor
   • Processing: approximately 4–6 weeks
3. Authorization granted?
   AIFA reviews and issues or requests clarification. Common issues: GMP certificate scope, product documentation, or AIFA queries about need given SCFM supply.
4. Italian Customs Entry
   EU customs procedures apply. Pharmaceutical-grade cannabis cleared for delivery to authorized importer.
   • AIFA import authorization (original)
   • All shipping documentation
   • EU customs narcotic declaration
5. Cleared for Italian Market ✓
   Pharmaceutical-grade cannabis released to authorized importer. QP release required before pharmacy supply.